6913 Remote jobs for English speakers in Europe

Senior Workday HR Reporting & Analytics Analyst owns and enhances Workday reporting, dashboards, and analytics. This role translates business questions into actionable workforce insights using Workday, Power BI, and modern data tools.

Senior Product Manager for Kimchi AI Coding Platform. Drive 0→1 product development in emerging AI/ML domains, turning ambiguity into clear product direction by exploring customer needs and technology shifts.

Lead and build the engineering capability for a major data platform transformation, overseeing data, analytics, and platform engineering. Own delivery, technical design, and establishing engineering standards.

Recruit internationally across all functions for a fast-growing AI tech company. Focus on tech talent, map top talent globally, and implement an AI-first recruitment stack. Requires 3+ years of recruitment experience, including 2 years in tech.

Seeking a driven Inside Sales Representative to manage the full remote sales cycle across the EU market. Responsibilities include lead qualification, remote demos, and driving revenue growth for tech solutions. Requires 1-3 years of B2B remote sales experience.

Lead global labeling strategy for CCDS, dCCDS, USPI, and EU SmPC. This senior role influences product development, ensures compliant labeling, and requires 10+ years of biotech/pharma experience.

Lead global labeling strategy for CCDS, dCCDS, USPI, and EU SmPC. This senior role influences product development, ensures compliant labeling, and requires 10+ years of biotech/pharma experience.

Lead global labeling strategy for CCDS, dCCDS, USPI, and EU SmPC. This senior role influences product development, ensures compliant labeling, and requires 10+ years of biotech/pharma experience.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.